53963-09-0Relevant articles and documents
PHEROMONES OF INSECTS AND THEIR ANALOGS XXXIII. SYNTHESIS OF HEXADEC-7Z,11E-DIEN-1-YL ACETATE - THE SEX PHEROMONE OF Sitotroga cerealella AND A COMPONENT OF THE SEX PHEROMONE OF Pectinophora gossypiella
Odinokov, V. N.,Ishmuratov, G. Yu.,Ladenkova, I. M.,Botsman, L. P.,Kargapol'tseva, T. A.,Tolstikov, G. A.
, p. 621 - 623 (2007/10/02)
From cyclohexene and caproaldehyde, using ozonolysis and the Knoevenagel reaction, we have synthesized hexadeca-7Z,11E-dien-1-yl acetate - the sex pheromone of Sitotroga cerealella and a component of the sex pheromone of Pectinophora gossypiella.
SHORT, REGIO- AND STEREO-SELECTIVE PREPARATION OF 1,5- AND 1,6-DIENES. SYNTHESES OF EUDIA PAVONIA PHEROMONE AND GOSSYPLURE.
Ducoux, Jean-Philippe,Menez, Patrick Le,Kunesch, Nicole,Kunesch, Gerhard,Wenkert, Ernest
, p. 2595 - 2598 (2007/10/02)
Two pheromones, (Z)-6,(Z)-11-hexadecadien-1-yl acetate (from Eudia pavonia) and gossyplure, have been synthesized each by two consecutive sequences of nickel-assisted Grignard reactions with cyclic enol ethers and the preparation of Grignard reagents from the resultant alcohols, followed each by copper-promoted Grignard reaction with a small-ring ether and subsequent acetylation.
4,8-Tridecadien-1-ol,4 cis,8 cis,trans
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, (2008/06/13)
Synthesis of the sex pheromone, (7Z,11Z/E)-7,11-hexadecadienyl acetate, of the pink bollworm moth, Pectinophora gossypiella, and intermediates therefor.